Similac Pro-Sensitive
Reason a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Recalled by Abbott Nutrition, Division of Abbott Laboratories · Columbus, OH, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Water filled bottles labeled as Similac Pro-Advance.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
Similac Pro-Advance Infant Formula with Iron, Milk-Based, Ready to Feed, 32 FL OZ (1 QT)
Quantity: 111 total cases.
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No lot or expiration date as bottles were not intended for distribution. Batch Numbers: BW3520316 (List Number 64248) and BW0970914 (List Number 66611).
Connecticut Maryland New Jersey New York Pennsylvania
FDA's distribution note: Products was distributed to the following states: CT, MD, NJ, NY, & PA.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
Reason a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Reason Product may be contaminated with Clostridium botulinum.
Reason Possible contamination with Cereulide toxin.
Reason Potential contamination with patulin.
Reason Contaminated with Clostridium botulinum